TY - JOUR
T1 - Downregulation of c-myc Expression after Heat Shock in Human B-Cell Lines Is Independent of 5’ mRNA Sequences
AU - Wennborg, Anders
AU - Classon, Marie
AU - Klein, George
AU - von Gabain, Alexander
N1 - Funding Information:
We thank P ivi Koskinen and Kari Alitalo for providing the hsp-myc construct. This work was supported by grants from NIH (5 RO1 CA14054) and the Swedish Cancer Society to G.K. and A. v. G.; by grants from the Swedish Society of Medicine and the Swedish Society for Medical Research to A.W.; and by grants fromtheAustrianScienceFoundationandtheJubil umsfondof the Austrian NationalBank to A.v.G.
PY - 1995
Y1 - 1995
N2 - The effect of heat-shock on the expression of c-myc genes in different chromosomal contexts was investigated in a panel of human B-lymphoid cell lines. Burkitt’s lymphoma cell lines with c-myc translocation breakpoints upstream of the first exon, within the exon itself, or in the first intron showed downregulation of c-myc levels as did a cell line without any translocation. The c-myc mRNA of cell lines with translocation breakpoints within the c-myc gene have previously been reported to have prolonged half-lives. After heat shock, the levels of these mRNA species were reduced with similar kinetics as the normal c-myc mRNA. An exception was an RNA species where the only c-myc sequences are derived from exon 1, showing that sequences from this part of the c-myc gene are not sufficient to mediate the rapid downregulation. Nuclear run-on analysis did not show reduced transcription of c-myc after heat shock and a comparison of cytoplasmic and total RNA did not indicate accumulation of longer, unspliced c-myc mRNA species. These observations suggest a posttranscriptional, cytoplasmic downregulation targeting exons 2 and/or 3. B-lymphoma lines transfected with a hsp70 promo-ter-linked c-myc gene were deficient in their ability to reinitiate proliferation after heat shock, providing a physiological rationale for the normal downregulation of c-myc after this type of physical stress.
AB - The effect of heat-shock on the expression of c-myc genes in different chromosomal contexts was investigated in a panel of human B-lymphoid cell lines. Burkitt’s lymphoma cell lines with c-myc translocation breakpoints upstream of the first exon, within the exon itself, or in the first intron showed downregulation of c-myc levels as did a cell line without any translocation. The c-myc mRNA of cell lines with translocation breakpoints within the c-myc gene have previously been reported to have prolonged half-lives. After heat shock, the levels of these mRNA species were reduced with similar kinetics as the normal c-myc mRNA. An exception was an RNA species where the only c-myc sequences are derived from exon 1, showing that sequences from this part of the c-myc gene are not sufficient to mediate the rapid downregulation. Nuclear run-on analysis did not show reduced transcription of c-myc after heat shock and a comparison of cytoplasmic and total RNA did not indicate accumulation of longer, unspliced c-myc mRNA species. These observations suggest a posttranscriptional, cytoplasmic downregulation targeting exons 2 and/or 3. B-lymphoma lines transfected with a hsp70 promo-ter-linked c-myc gene were deficient in their ability to reinitiate proliferation after heat shock, providing a physiological rationale for the normal downregulation of c-myc after this type of physical stress.
KW - Heat-shock
KW - Post-transcriptional regulation
KW - c-myc Chromosomal translocation
UR - http://www.scopus.com/inward/record.url?scp=0029410760&partnerID=8YFLogxK
U2 - 10.1515/bchm3.1995.376.11.671
DO - 10.1515/bchm3.1995.376.11.671
M3 - Article
C2 - 8962676
AN - SCOPUS:0029410760
SN - 0177-3593
VL - 376
SP - 671
EP - 680
JO - Biological Chemistry Hoppe-Seyler
JF - Biological Chemistry Hoppe-Seyler
IS - 11
ER -